Zhang Jing, Yan Shuai, He Zhiyong, Ding Cong, Zhai Tianxing, Chen Yage, Li Haozheng, Yang Guang, Zhou Xiang, Wang Ping
Britton Chance Center for Biomedical Photonics , Wuhan National Laboratory for Optoelectronics-Huazhong University of Science and Technology , Wuhan , Hubei 430074 , China.
MoE Key Laboratory for Biomedical Photonics, Collaborative Innovation Center for Biomedical Engineering, School of Engineering Sciences , Huazhong University of Science and Technology , Wuhan , Hubei 430074 , China.
J Phys Chem Lett. 2018 Aug 16;9(16):4679-4685. doi: 10.1021/acs.jpclett.8b01991. Epub 2018 Aug 3.
Raman has been implemented to image biological systems for decades. However, Raman microscopy along with Raman probes is restricted to image metabolites or a few intracellular organelles so far and lacks genetic specificity for imaging proteins of interest, which significantly hinders their application. Here, we report the Raman spectra-based protein imaging method, which incorporates a small phenyl ring enhanced Raman tag (total of ∼0.55 kDa) with a single unnatural amino acid (UAA) to genetically label specific proteins. We further demonstrate hyperspectral stimulated Raman scattering (SRS) imaging of the Histone3.3 protein in the nucleus, Sec61β protein in the endoplasmic reticulum of HeLa cells, and Huntingtin protein Htt74Q in mutant huntingtin-induced cells. Genetic encoding of a small, stable, sensitive, and narrow-band Raman tag took one key step forward to enable SRS or Raman imaging of specific proteins and could further facilitate quantitative Raman spectra-based supermultiplexing microscopy in the future.
几十年来,拉曼光谱已被用于生物系统成像。然而,到目前为止,拉曼显微镜结合拉曼探针仅限于对代谢物或少数细胞内细胞器进行成像,并且缺乏对感兴趣蛋白质成像的遗传特异性,这严重阻碍了它们的应用。在此,我们报告了一种基于拉曼光谱的蛋白质成像方法,该方法将一个带有单个非天然氨基酸(UAA)的小苯环增强拉曼标签(总计约0.55 kDa)整合在一起,用于对特定蛋白质进行基因标记。我们进一步展示了对细胞核中的组蛋白3.3、HeLa细胞内质网中的Sec61β蛋白以及突变型亨廷顿蛋白诱导细胞中的亨廷顿蛋白Htt74Q进行高光谱受激拉曼散射(SRS)成像。一个小的、稳定的、灵敏的和窄带拉曼标签的基因编码向前迈出了关键一步,实现了对特定蛋白质的SRS或拉曼成像,并可能在未来进一步推动基于拉曼光谱的定量超多重显微镜技术发展。